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Afternoon Production Laboratory Technician (6-Month Contract)

CEVA SANTE ANIMALE

Guelph

On-site

CAD 45,000 - 55,000

Full time

7 days ago
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Job summary

A global leader in animal health is seeking an Afternoon Production Laboratory Technician for a 6-month contract in Guelph, Ontario. This role focuses on vaccine production, ensuring compliance with quality and safety standards while managing daily laboratory activities. The ideal candidate has post-secondary education and experience in a lab or GMP setting. Join a passionate team committed to improving animal health and fostering a diverse workplace.

Qualifications

  • Previous experience in a lab or GMP manufacturing environment preferred.
  • Experience working with bioreactors is a plus.

Responsibilities

  • Conduct manufacturing operations complying with HSE standards.
  • Manage production and ensure workspace organization.
  • Participate in documentation system construction and validation processes.

Skills

Laboratory procedures
GMP compliance
Problem solving
Teamwork

Education

Post-secondary education in a related field

Job description

Afternoon Production Laboratory Technician (6-Month Contract)

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Afternoon Production Laboratory Technician (6-Month Contract)

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The success of a company depends on the passionate people we partner with.

Together, let's share our talents.

As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.

We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.

Indeed, Our “Together, Beyond Animal Health” vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.

As part of our “Diversity, Equity and Inclusion” policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.

Your Missions

Afternoon Production Laboratory Technician

6-Month Contract

This role is on the afternoon shift which is Monday-Friday 2 : 00PM - 10 : 00PM.

The Vaccine production operator carries out manufacturing operations in accordance with appropriate procedures, in compliance with HSE standards, productivity targets and quality standards (GMP, hygiene). Propose ideas to improve productivity and they own their environment (workstations organization, quality and safety).

The operator will propose ideas to improve productivity and take accountability for their workspace He / she is responsible for the daily activities of the laboratory and ensures they meet the appropriate specifications for the production of animal vaccines (harvesting, purification and aseptic filling activities).

The Vaccine production operator will participate in the construction of the new documentation system and the validation of the equipment and processes (clean zone, autoclaves, centrifuge, tangential flow filtration system).

Duties Include

Managing Production

Day To Week

  • Suggest set-up of the team’s work in daily Tier 1 based on the given production schedule.
  • Execute production planning, reporting quality standards.
  • Inform & escalate in case of issue or in case can’t solve / deviation.
  • Monitor & improve his activity on continuous basis.
  • Close & control work orders.
  • Complete the processing, documentation and cleaning in an aseptic processing area.
  • Work independently, complete daily tasks accurately and efficiently.
  • Collect samples from various tanks, surfaces and environment.
  • Perform equipment and instrument calibrations according to established procedures.
  • Identify and report irregularities identified with any aspects of work.
  • Review production batch records.

Budget & Cost Control

  • Respect operating time yield standards.
  • Analyze some variances and propose implementation of action plans.
  • Compliance and Safeguard

  • Set-up / write SOP’s.
  • Apply all standards (environment, quality, safety / HSE, aseptic, cost).
  • Perform In-Process Controls (IPC).
  • Complete and check batch reports.
  • Raise alert in case of dangerous situations, near miss / miss, QA deviation etc.
  • Run internal audits.
  • Participate in writing new SOP and Batch Production Records.
  • Ensures 5S standards are met and maintained.
  • Follows all health and safety rules and regulations.
  • Participate in the validation process with guidance.
  • Operational Excellence : Continuous Improvement

  • On the assigned workstations, ensure that CPS standards are applied.
  • Update & monitor performance indicators on his / her line / zone, analyse gaps, propose and perform resolution actions.
  • Propose and implement ideas for improvement (short / medium term).
  • Carry out process confirmation as provided by the corresponding planning function.
  • Guarantee compliance with performance and workshop storage standards in the assigned workshops; raise alert if needed.
  • Maintenance

  • Ensure first level of maintenance and changeovers (=clean machines and keep them in good condition), escalate if any deviation / issue.
  • Act as a responder for incoming spill calls. Be part of the spill response team.
  • Long / Mid Term Strategy, CAPEX

  • Suggest small CAPEX investments to improve performance (below 5K€).
  • Project Management

  • Actively participate in occasional site / department projects and in continuous improvement workshops.
  • Management

  • Share good practices.
  • Train temporary workers and / or junior operators.
  • Own personal development : know skill matrix and suggest training to supervisor.
  • Perform other duties as assigned.
  • Your Profile

    About You :

  • You have a post-secondary education in a related field
  • Ideally, you have previous experience in a lab or GMP manufacturing environment
  • Ideally, you have previous experience working with bioreactors
  • Seniority level

    Seniority level

    Not Applicable

    Employment type

    Employment type

    Contract

    Job function

    Job function

    Research, Analyst, and Information Technology

    Industries

    Pharmaceutical Manufacturing

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